Frequency of common HFE variants in the Saudi population: a high throughput molecular beacon-based study

BACKGROUND: Hereditary Hemochromatosis (HH) is an autosomal recessive disorder highlighted byiron-overload. Two popular mutations in HFE, p.C282Y and p.H63D, have been discovered and found to associate with HH in different ethnic backgrounds. p.C282Y and p.H63D diagnosis is usually made byrestrictio...

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Detaylı Bibliyografya
Asıl Yazarlar: Alsmadi, Osama A, Al-Kayal, Fadi, Al-Hamed, Mohamed, Meyer, Brian F
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2006
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1468397/
https://ncbi.nlm.nih.gov/pubmed/16672055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-7-43
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